Henny-Harry C, Trotman H
Department of Child and Adolescent Health, The University of the West Indies, Kingston 7, Jamaica, West Indies.
West Indian Med J. 2012 Jan;61(1):37-42.
To describe the epidemiology of neonatal jaundice at the University Hospital of the West Indies (UHWI).
A retrospective review of all neonates at the UHWI with clinically significant jaundice between January 1, 2006 and June 30, 2007 was performed. Demographic, clinical and laboratory data were collected. Descriptive analyses were performed.
The incidence of clinically significant neonatal jaundice at the UHWI was 4.6% for the study period. There were 103 male (61%) and 67 (39%) female infants. The aetiology ofjaundice in the infant was attributed to ABO incompatibility in 59 (35%), infection in 30 (18%), prematurity in 19 (11%), G6PD deficiency in 8 (5%), Rhesus incompatibility in 6 (3.5%) and no cause was identified in 16 (9%) infants. There was a low incidence (26%) ofscreening for G6PD deficiency although it was the most common aetiology for infants presenting from home. Nine (5%) neonates required exchange blood transfusion. Infants admitted from home had a significantly higher mean total bilirubin value at presentation, a significantly higher mean peak bilirubin level andpresented significantly later than those who were admitted from the postnatal ward (p < 0.001). One patient was discharged with a diagnosis of bilirubin encephalopathy but defaulted from follow-up. Two neonates died but from causes unrelated to neonatal jaundice. Sixty-two patients (37%) were followed-up post discharge; 50% had hearing tests done, all tests were normal. Sixty-one (98%) infants had normal development at the time of the study; one patient had impaired motor development but this infant also had a myelomeningocoele.
To further reduce morbidity associated with neonatal jaundice at the UHWI, there should be increased screening for G6PD deficiency; current systems in place for follow-up and monitoring of infants discharged from hospital prior to 72 hours must also be expanded and strengthened.
描述西印度群岛大学医院(UHWI)新生儿黄疸的流行病学情况。
对UHWI在2006年1月1日至2007年6月30日期间所有患有具有临床意义黄疸的新生儿进行回顾性研究。收集人口统计学、临床和实验室数据,并进行描述性分析。
在研究期间,UHWI具有临床意义的新生儿黄疸发病率为4.6%。有103名男婴(61%)和67名女婴(39%)。婴儿黄疸的病因归因于ABO血型不合的有59例(35%),感染的有30例(18%),早产的有19例(11%),葡萄糖-6-磷酸脱氢酶(G6PD)缺乏的有8例(5%),Rh血型不合的有6例(3.5%),16例(9%)婴儿未查明病因。G6PD缺乏症的筛查率较低(26%),尽管它是在家中就诊婴儿最常见的病因。9名(5%)新生儿需要换血治疗。在家中入院的婴儿入院时平均总胆红素值显著更高,平均胆红素峰值水平显著更高,且入院时间显著晚于从产后病房入院的婴儿(p < 0.001)。1例患者出院时诊断为胆红素脑病,但失访。2名新生儿死亡,但死因与新生儿黄疸无关。62例患者(37%)出院后接受了随访;50%进行了听力测试,所有测试均正常。在研究时,61例(98%)婴儿发育正常;1例患者运动发育受损,但该婴儿也患有脊髓脊膜膨出。
为进一步降低UHWI与新生儿黄疸相关的发病率,应增加对G6PD缺乏症的筛查;目前对72小时前出院婴儿的随访和监测系统也必须扩大和加强。